Prenatal detection of an inherited Duchenne muscular dystrophy deletion allele-Reference-Cited by-同舟云学术

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Prenatal detection of an inherited Duchenne muscular dystrophy deletion allele

Published:1987-02-01 Issue:2 Volume:37 Page:355-355
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Bartlett R. J.,Pericak-Vance M. A.,Lanman J. T.,Killam A. P.,Gilbert J. R.,Stajich J. M.,Chen J. C.,Siddique T.,Kandt R. S.,Sirotkin-Roses M.,Roses A. D.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Duchenne muscular dystrophy:detection of deletion carriers by spectrophotometric densitometry;Clinical Genetics;2008-06-28

2. Investigation of muscle disease.;Journal of Neurology, Neurosurgery & Psychiatry;1996-03-01

3. Verification of carrier status for Becker muscular dystrophy from analysis of a blighted ovum;Prenatal Diagnosis;1993-08

4. Molecular genetics and genetic counselling for Duchenne/Becker muscular dystrophy;Molecular and Cell Biology of Muscular Dystrophy;1993

5. Identification of duchenne muscular dystrophy genomic probe P20 constant Taq1 fragment corresponding to the EcoRV and Msp1 polymorphisms;Prenatal Diagnosis;1991-01

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